ß-Spectrin São PauloII, a novel frameshift mutation of the ß-spectrin gene associated with hereditary spherocytosis and instability of the mutant mRNA-Reference-Cited by-同舟云学术

ß-Spectrin São PauloII, a novel frameshift mutation of the ß-spectrin gene associated with hereditary spherocytosis and instability of the mutant mRNA

Published:2002-08 Issue:8 Volume:35 Page:921-925
ISSN:0100-879X
Container-title:Brazilian Journal of Medical and Biological Research
language:
Short-container-title:Braz J Med Biol Res

Author:

Bassères D.S.¹,Tavares A.C.²,Costa F.F.³,Saad S.T.O.³

Affiliation:

1. Universidade Estadual de Campinas; Universidade Estadual de Campinas, Brasil

2. Universidade Estadual de Campinas

3. Universidade Estadual de Campinas; Universidade Estadual de Campinas

Publisher

FapUNIFESP (SciELO)

Subject

Cell Biology,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Immunology,Physiology,Biochemistry,General Neuroscience,Biophysics

Link

http://www.scielo.br/pdf/bjmbr/v35n8/4595.pdf

Reference20 articles.

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3. Red blood cell membrane disorders;Tse WT;British Journal of Haematology,1999

4. ß-spectrin Kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1;Becker PS;Journal of Clinical Investigation,1993

5. Molecular basis of spectrin deficiency in ß spectrin Durham;Hassoun H;Journal of Clinical Investigation,1995

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3. Spectrins in Human Diseases;Cytoskeleton and Human Disease;2012

4. Novel beta-spectrin mutations in hereditary spherocytosis associated with decreased levels of mRNA;British Journal of Haematology;2009-08